MovDisordV3, Main, Exploration, bibRecord, 004773

Intrafamilial heterogeneity of facial hyperkinesias: Chance association of tics, cranial dystonia, and Huntington's disease?

Identifieur interne : 004773 ( Main/Exploration ); précédent : 004772; suivant : 004774

Intrafamilial heterogeneity of facial hyperkinesias: Chance association of tics, cranial dystonia, and Huntington's disease?

Auteurs : Jörg Müller [Autriche] ; Gregor K. Wenning [Autriche] ; Jörg Wissel [Autriche] ; Werner Poewe [Autriche]

Source :

Movement Disorders [ 0885-3185 ] ; 2001-03.

RBID : ISTEX:8A36A6F17C87F1AF79F895E6B75C88720F73CE4A

Descripteurs français

Pascal (Inist)
- Adulte, Chorée Huntington, Diagnostic différentiel, Dystonie, Etude familiale, Face, Hyperkinésie, Hétérogénéité, Mâle, Phénotype, Tic.
Wicri :
- topic : Adulte.

English descriptors

KwdEn :
- Adult, Atrophy (pathology), Caudate Nucleus (metabolism), Caudate Nucleus (pathology), Cognition Disorders (diagnosis), Cognition Disorders (etiology), Corpus Striatum (metabolism), Corpus Striatum (pathology), Differential diagnostic, Dopamine (metabolism), Dystonia, Dystonic Disorders (complications), Dystonic Disorders (genetics), Face, Facial Muscles (physiopathology), Family study, Heterogeneity, Humans, Huntington Disease (complications), Huntington Disease (diagnosis), Huntington Disease (genetics), Huntington disease, Hyperkinesia, Hyperkinesis (genetics), Hyperkinesis (physiopathology), Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Phenotype, Skull, Tic, Tic Disorders (complications), Tic Disorders (genetics), Tomography, Emission-Computed, Single-Photon, Trinucleotide Repeats (genetics).
MESH :
- chemical , metabolism : Dopamine.
- complications : Dystonic Disorders, Huntington Disease, Tic Disorders.
- diagnosis : Cognition Disorders, Huntington Disease.
- etiology : Cognition Disorders.
- genetics : Dystonic Disorders, Huntington Disease, Hyperkinesis, Tic Disorders, Trinucleotide Repeats.
- metabolism : Caudate Nucleus, Corpus Striatum.
- pathology : Atrophy, Caudate Nucleus, Corpus Striatum.
- physiopathology : Facial Muscles, Hyperkinesis.
- Adult, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Skull, Tomography, Emission-Computed, Single-Photon.

Url:

https://api.istex.fr/document/8A36A6F17C87F1AF79F895E6B75C88720F73CE4A/fulltext/pdf

DOI: 10.1002/mds.1058

Affiliations:

Le document en format XML

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<term>Cognition Disorders (diagnosis)</term>
<term>Cognition Disorders (etiology)</term>
<term>Corpus Striatum (metabolism)</term>
<term>Corpus Striatum (pathology)</term>
<term>Differential diagnostic</term>
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<term>Trinucleotide Repeats (genetics)</term>
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<term>Trinucleotide Repeats</term>
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Movement Disorders (revue)

Intrafamilial heterogeneity of facial hyperkinesias: Chance association of tics, cranial dystonia, and Huntington's disease?

Intrafamilial heterogeneity of facial hyperkinesias: Chance association of tics, cranial dystonia, and Huntington's disease?

Source :

Descripteurs français

English descriptors

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.